电催化剂
多硫化物
氧化还原
材料科学
电池(电)
电化学
纳米技术
对偶(语法数字)
储能
硫黄
化学工程
电极
电解质
阴极
化学
物理化学
热力学
物理
文学类
工程类
艺术
功率(物理)
冶金
作者
Zixiong Shi,Zhongti Sun,Jingsheng Cai,Xianzhong Yang,Chaohui Wei,Menglei Wang,Yifan Ding
标识
DOI:10.1002/adma.202103050
摘要
Lithium-sulfur (Li-S) batteries are promising candidates for next-generation energy storage, yet they are plagued by the notorious polysulfide shuttle effect and sluggish redox kinetics. While rationally designed redox mediators can facilitate polysulfide conversion, favorable bidirectional sulfur electrocatalysis remains a formidable challenge. Herein, selective dual-defect engineering (i.e., introducing both N-doping and Se-vacancies) of a common MoSe2 electrocatalyst is used to manipulate the bidirectional Li2 S redox. Systematic theoretical prediction and detailed electrokinetic analysis reveal the selective electrocatalytic effect of the two types of defects, thereby achieving a deeper mechanistic understanding of the bidirectional sulfur electrochemistry. The Li-S battery using this electrocatalyst exhibits excellent cyclability, with a low capacity decay rate of 0.04% per cycle over 1000 cycles at 2.0 C. More impressively, the potential for practical applications is highlighted by a high areal capacity (7.3 mAh cm-2 ) and the construction of a flexible pouch cell. Such selective electrocatalysis created by dual-defect engineering is an appealing approach toward working Li-S systems.
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